{{Rsnum
|rsid=63750206
|Chromosome=3
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=MLH1
|position=36996701
|Gene_s=MLH1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A,T
|CHROM=3
|CLNACC=RCV000075474.1; RCV000018618.26; RCV000018619.26; RCV000075475.1
|CLNALLE=1; 2
|CLNDBN=Lynch syndrome; Lynch syndrome II; Turcot syndrome
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005; NBK1211:C1333991:609310:144; NBK1211:C0265325:276300:252202:61665008
|CLNHGVS=NC_000003.11:g.37038192G>A; NC_000003.11:g.37038192G>T
|CLNORIGIN=1
|CLNSRC=InSiGHT; OMIM Allelic Variant
|CLNSRCID=c.199G>A; c.199G>T; 120436.0011
|Disease=Lynch syndrome; Lynch syndrome II; Turcot syndrome
|FwdALT=A,T
|FwdREF=G
|GENEINFO=MLH1:4292
|GENE_ID=4292
|GENE_NAME=MLH1
|REF=G
|RSPOS=37038192
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=63750206
|CLNSIG=5
}}